Mercurial > repos > nick > duplex
annotate duplex.xml @ 5:9d46c9ca7ceb draft
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| author | nick |
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| date | Mon, 23 Nov 2015 18:46:22 -0500 |
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| children | e504cc1d5a76 |
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1 <?xml version="1.0"?> |
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2 <tool id="duplex" name="Make consensus reads" version="0.1"> |
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3 <description>from duplex sequencing data</description> |
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4 <requirements> |
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5 <requirement type="package" version="0.1">duplex</requirement> |
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6 </requirements> |
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7 <command interpreter="python" detect_errors="exit_code"><![CDATA[ |
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8 duplex.py -r $min_reads -q $qual_thres -F $qual_format $input |
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9 #if $keep_sscs: |
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10 --sscs-file $sscs |
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11 #end if |
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12 > duplex.fa |
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13 && awk -f $__tool_directory__/utils/outconv.awk -v target=1 duplex.fa > $output1 |
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14 && awk -f $__tool_directory__/utils/outconv.awk -v target=2 duplex.fa > $output2 |
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15 ]]> |
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16 </command> |
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17 <inputs> |
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18 <param name="input" type="data" format="tabular" label="Aligned input reads" /> |
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19 <param name="min_reads" type="integer" value="3" min="1" label="Minimum reads per family" help="Single-strand families with fewer than this many reads will be skipped."/> |
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20 <param name="qual_thres" type="integer" value="25" min="1" label="Minimum base quality" help="Bases with a PHRED score less than this will not be counted in the consensus making."/> |
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21 <param name="qual_format" type="select" label="FASTQ format" help="Solexa should also work for Illumina 1.3+ and 1.5+, and Sanger should work for Illumina 1.8+"> |
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22 <option value="sanger" selected="true">Sanger (PHRED 0 = "!")</option> |
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23 <option value="solexa">Solexa (PHRED 0 = "@")</option> |
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24 </param> |
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25 <param name="keep_sscs" type="boolean" truevalue="true" falsevalue="" label="Output single-strand consensus sequences" /> |
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26 </inputs> |
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27 <outputs> |
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28 <data name="output1" format="fasta" label="$tool.name on $on_string (mate 1)"/> |
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29 <data name="output2" format="fasta" label="$tool.name on $on_string (mate 2)"/> |
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30 <data name="sscs" format="fasta" label="$tool.name on $on_string (SSCS)"> |
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31 <filter>keep_sscs</filter> |
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32 </data> |
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33 </outputs> |
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34 <help> |
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35 |
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36 **What it does** |
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37 |
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38 This is for processing duplex sequencing data. It creates single-strand and duplex consensus reads from aligned read families. |
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39 |
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40 ----- |
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41 |
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42 **Input** |
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43 |
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44 This expects the output format of the "Align families" tool. |
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45 |
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46 ----- |
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47 |
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48 **Output** |
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49 |
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50 This will output final, duplex consensus reads in two FASTA files (first and second reads in the pairs). Optionally, you can save the single-strand reads too, in a separate FASTA file. |
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51 |
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52 </help> |
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53 </tool> |
